BEUDAMED
    FDA Registration Active 🇺🇸 United States

    IntelliVue CL Respiration Pod, SW Rev. B

    Reg #: 3016618143 · FEI: 3016618143 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    6
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Philips North America LLC
    Registration Number
    3016618143
    FEI Number
    3016618143
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    222 Jacobs Street
    City
    Cambridge
    State
    MA
    ZIP
    02141
    Country
    US

    Regulatory Submissions

    510(k) Number
    K122223

    Owner / Operator

    Firm Name
    Philips Medical Systems International BV
    Operator Number
    1217116
    Address
    Veenpluis 6
    City
    Best
    State
    NL-NOTA
    Postal Code
    5684PC
    Country
    NL

    Products

    Device Name Product Code
    Monitor, Breathing Frequency BZQ

    Proprietary Names

    IntelliVue CL Respiration Pod, SW Rev. B IntelliVue GuardianSoftware SW Rev. A2 IntelliVue Patient Monitor MP2, SW Rev. J7 IntelliVue Patient Monitor MP5, MP5T, MP5SC, SW Rev. J7 IntelliVue Multi-Measurement Module X2, SW Rev. J7 989803179541 Mobile CL Respiration Pod Attachment

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198